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Building Empowerment and Coping Outcomes for CaNcer Patients, Survivors and Their Caregivers

BEACON Study: Virtual Coping Skills Groups for Cancer Patients, Survivors and Their Caregivers

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06353178
Acronym
BEACON
Enrollment
133
Registered
2024-04-08
Start date
2024-04-08
Completion date
2025-01-25
Last updated
2025-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer, Caregiver Burnout, Caregiving Stress, Survivorship

Keywords

cancer, caregiving, emotional support, psychology

Brief summary

Cancer has a psychological, emotional and social impact beyond a patient's physical health. This study examines three new online peer mental-wellness support program for cancer patients, survivors or their caregivers. Each program teaches evidence-based skills, in the context of that groups lived experience, to manage the emotional impact of cancer. This study examines the impact of that program.

Detailed description

Cancer has a psychological, emotional and social impact beyond a patient's physical health. These problems often ripple beyond the individual with the diagnosis, to their broader community, and also beyond a cancer treatment course into survivorship. As a result, there are a wide range of socioemotional needs in those who have been impacted by cancer. Further, these emotional impacts have a direct impact on morbidity and mortality of cancer. A new peer mental-wellness support program, called Color Cancer Connect (CCC) supports cancer patients, survivors and their caregivers by teaching them evidence-based skills to manage the emotional impact of cancer. This study will examine all three programs (i.e., patient, survivor, caregiver) to gather data to measure the impact of the program on emotional well-being, quality of life and health behaviors.

Interventions

BEHAVIORALCancer Connect Program

Online group peer program where participants learn evidence based skills for managing stressors and emotions related to their cancer experience.

Sponsors

Color Health, Inc.
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Masking description

Participants will be notified of a waitlist assignment upon enrolling. Those on the waitlist will receive the intervention after 3 months.

Intervention model description

Participants will be randomized to waitlist or intervention group. Those in intervention group will receive the peer program; those on the waitlist will receive it after being on the waitlist for 3 months.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Lived experience as either a current cancer patient, cancer survivor or caregiver of someone with cancer * Adult - 18+ * Has health insurance provided by employer or union (can be dependent of person on insurance) * Read/speak English * Have access to internet and personal email account

Exclusion criteria

* Severe mental illness that is disruptive to other group members

Design outcomes

Primary

MeasureTime frameDescription
DepressionMultiple time points across 8 months (waitlist; baseline, 2 months post waitlist, 3 months post waitlist, 2 months post program start, 3 months post program start) or 5 months (intervention; baseline, 2 months post program start, 3 months post program)Patient Health Questionnaire-9 (PHQ-9)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026